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CRHR1 变体与自杀未遂中的身体攻击之间的基因-环境相互作用。

Gene-environment interactions between CRHR1 variants and physical assault in suicide attempts.

机构信息

Department of Public Health Sciences, The National Prevention of Suicide and Mental Ill-Health (NASP), Karolinska Institute (KI), Stockholm, Sweden.

出版信息

Genes Brain Behav. 2011 Aug;10(6):663-72. doi: 10.1111/j.1601-183X.2011.00703.x. Epub 2011 Jun 9.

Abstract

Risk factors for suicidal behaviors are partly heritable, including genetic variants that drive diathesis-stress in addition to, or by interaction with, exposure to certain stressful life events (SLEs). Hypothalamic-pituitary-adrenal (HPA) axis regulatory genes are candidates for association with suicide as well as its endophenotypes. Using a family-based design of offspring who attempted suicide (SA) and both parents, we investigated gene-environment interactions (G×Es) of SLE exposures with single nucleotide polymorphisms (SNPs) in corticotropin-releasing hormone receptor-1 (CRHR1), a major HPA axis regulatory gene. We observed a novel G×E among predominantly female SA between 5'-SNP rs7209436 and childhood/adolescence physical assault or attack (PA), as well as a second novel and male-specific G×E between 3'-SNP rs16940665 and adulthood PA exposure. A third male-specific G×E previously reported by us among depressed SA, between SNP rs4792887 and cumulative SLEs, was also further confirmed. The two novel G×Es presented here shared the SA characteristic of aggression, while showing differences on other aspects of SA heterogeneity. We conclude that different SA subjects were observed to differentially associate with two novel G×Es involving exposures to PA with different life timing and SNPs located in opposite ends of CRHR1. Concerning sex differences, we observed three subsets of distinct male SA that associated with each of the three observed G×Es, whereas female SAs were affected by only one of the G×Es. These results are consistent with a diathesis-stress model of suicidal behavior and may help to explain SA heterogeneity.

摘要

自杀行为的风险因素部分是遗传的,包括除了与特定的生活应激事件(SLEs)暴露相互作用之外,还驱动素质-应激的遗传变异。下丘脑-垂体-肾上腺(HPA)轴调节基因是与自杀及其表型相关的候选基因。我们使用自杀未遂(SA)的后代及其父母的基于家庭的设计,研究了 HPA 轴调节基因促肾上腺皮质激素释放激素受体 1(CRHR1)中的单核苷酸多态性(SNP)与 SLE 暴露的基因-环境相互作用(G×E)。我们观察到一个新的 G×E,主要是女性 SA 中 5'-SNP rs7209436 与童年/青春期的身体攻击或攻击(PA)之间,以及第二个新的和男性特异性的 G×E 之间 3'-SNP rs16940665 与成年 PA 暴露之间。我们之前报道的另一个男性特异性 G×E 也在抑郁 SA 之间的 SNP rs4792887 和累积 SLE 之间进一步证实。这里提出的两个新的 G×E 与具有攻击性的 SA 特征共享,同时在 SA 异质性的其他方面表现出差异。我们得出结论,不同的 SA 个体被观察到与涉及不同生活时间的 PA 暴露和位于 CRHR1 相反末端的 SNP 的两个新的 G×E 不同地相关。关于性别差异,我们观察到三个不同的男性 SA 子集与三个观察到的 G×E 中的每一个相关,而女性 SA 仅受一个 G×E 的影响。这些结果与自杀行为的素质-应激模型一致,可能有助于解释 SA 异质性。

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